Canonical Allele Identifier: PA1139717729
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 947124
ClinVar RCV Id: RCV001218125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036342.2:p.Glu19Gln
CA5210895
NM_012210.3:c.55G>C